O

Opella

Global OTC & VMS self-care manufacturer

Medical Information and Medical Compliance Manager

Regulatory & Quality (Life Sciences)Posted on Nov 14
Full-timeShanghai, ChinaNo salary listedIn-person

About the Job

Requirements

  • Maintain compliance with relevant company, industry, legal, and regulatory requirements.
  • Build strong cross-functional relationships with colleagues in Medical Affairs, Clinical Affairs, and Commercial Operations.

Responsibilities

  • Set up and manage Opella China’s Medical Information operational system in compliance with global and local, internal and external requirements.
  • Create and maintain response documents.
  • Train the Contact Center on Opella-specific products and topics.
  • Conduct quality checks of Opella-related inquiries.
  • Manage and respond to escalations of medical inquiries.
  • Manage Opella-specific local Medical Information phone numbers.
  • Provide Medical Information input to launch teams and crisis teams, and coordinate related activities.
  • Develop and test Opella-specific system requirements.
  • Provide input into product dictionaries for Opella products in the system.
  • Generate metrics, reports, dashboards, and insights.
  • Provide Medical Information input to business development activities, including product divestments and acquisitions.
  • Manage specific quality documents.
  • Manage and contribute to relevant audits and inspections.
  • Represent Medical Information at conferences and perform other local Medical Information activities.
  • Arrange systematic training plans for the Opella China Medical team and role-specific training plans, including onboarding, compliance, medical capabilities, internal systems, guidance and standard operating procedures, disease and product knowledge, internal and external medical GxP, and general capabilities and skills training; ensure execution is arranged and tracked.
  • Establish the medical compliance operational system and processes for Opella China, and provide operational compliance guidance for medical, marketing, and medico-marketing activities.
  • Absorb responsibilities transferred from the Medical Excellence/BOS team, particularly support for the EET process workflow.
  • Ensure a clear review process for Medical-related programs and activities before final approval, including Medical Education Meetings, Advisory Board Meetings, Steering Committees, sponsorships, partnerships, Patient Support Programs, Market Research programs, and Medical Liaison programs and activities.

About the Company

Opella

Global OTC & VMS self-care manufacturer

Opella makes a wide range of over-the-counter medicines, vitamins, minerals, and supplements for global consumers, covering about 100 brands and an 11,000-strong workforce. It develops, manufactures, and markets non-prescription health products that people can buy ready-made in stores for common needs such as pain relief, digestion, and allergy relief. The company differentiates itself with a large global manufacturing footprint (13 sites and 4 science and innovation centers) and its B Corp certification, signaling accountability to social and environmental standards. Its goal is to simplify self-care and put health in people’s hands for half a billion consumers worldwide.

Company size
5,001-10,000
Company stage
Not listed
Total funding
Not listed
Headquarters
Neuilly-sur-Seine, France
Founded
2018

Recently Posted Jobs

Explore more opportunities at Opella

See more jobs